zoledronic acid
Generic: zoledronic acid
Labeler: gland pharma limitedDrug Facts
Product Profile
Brand Name
zoledronic acid
Generic Name
zoledronic acid
Labeler
gland pharma limited
Dosage Form
INJECTION
Routes
Active Ingredients
zoledronic acid 5 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
68083-256
Product ID
68083-256_a8e4a749-32b9-41fd-8dbc-9451e97cf001
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209578
Listing Expiration
2027-12-31
Marketing Start
2017-03-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68083256
Hyphenated Format
68083-256
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
zoledronic acid (source: ndc)
Generic Name
zoledronic acid (source: ndc)
Application Number
ANDA209578 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/100mL
Packaging
- 1 BAG in 1 CARTON (68083-256-01) / 100 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a8e4a749-32b9-41fd-8dbc-9451e97cf001", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["705824"], "spl_set_id": ["d761011b-edd6-4d3f-bacd-8607dc2414fc"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 CARTON (68083-256-01) / 100 mL in 1 BAG", "package_ndc": "68083-256-01", "marketing_start_date": "20170313"}], "brand_name": "Zoledronic acid", "product_id": "68083-256_a8e4a749-32b9-41fd-8dbc-9451e97cf001", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68083-256", "generic_name": "Zoledronic acid", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "5 mg/100mL"}], "application_number": "ANDA209578", "marketing_category": "ANDA", "marketing_start_date": "20170313", "listing_expiration_date": "20271231"}